Evaluate the Efficacy of an Oral Health Behavioral Intervention in People With Diabetes

Part of paid clinical trials in Long Island City, New York.

Sponsor
Colgate Palmolive
Study ID
NCT07619729
Phase
PHASE4
Status
Enrolling By Invitation

Conditions

  • Caries
  • Diabetes Type 2
  • Periodontal Disease

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Diabetes Oral Health Program — BEHAVIORAL
    All subjects will receive a behavioral intervention through text messages with links to educational pages about oral health or diabetes. Subjects will have the option of selecting in to the product intervention.
  • Stannous Fluoride Dentifrice — DRUG
    This is an opt-in product intervention, and it is expected that not all subjects will opt-in. Subjects will need to re-order the product every 3 months. All subjects who order product will receive a toothbrush, toothpaste, and mouthwash.
  • Cetylpyridinium Chloride (CPC) and Zinc Lactate Mouthwash — DRUG
    This is an opt-in product intervention, and it is expected that not all subjects will opt-in. Subjects will need to re-order the product every 3 months. All subjects who order product will receive a toothbrush, toothpaste, and mouthwash.

Study Details

The purpose of this clinical study is to evaluate the effect of a behavioral intervention on the number of preventive and treatment dental claims in a population of people with Type 2 Diabetes.

Key Dates

Start date
May 26, 2026
Status verified
May 2026
Primary completion
Jan 2, 2028
Completion
Jan 2, 2028

Study Design

Enrollment
10,000 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION

Arms

  • Experimental: Type 2 Diabetes
    This is a single-group study. All subjects will be enrolled in the experimental group.

Primary Outcome Measure

Dental Claims [ Time Frame: 12 months ]

Locations (1)

FacilityCityStateZIPSite coordinators
Decentralized Site - Virtual/Remote (NY, USA)Long Island CityNew York11101-

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